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HRID 225274作成日:2026年10月26日

Dimethylformamide → 7-[3-(Trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrile

https://huagongshe.com/reaction/225274

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物3-Bromo-7-(alpha,alpha,alpha-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidineHCID 11473317—
生成物7-[3-(Trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 2741014—

反応手順

A mixture of 0.95 g. of 3-bromo-7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine, 0.45 g. cuprous cyanide and 25 ml. of dimethylformamide is refluxed for 16 hours. Evaporation of the reaction mixture gave a residue which was triturated with methylene chloride. The methylene chloride solution is passed through a short column of hydrous magnesium silicate. The effluent is collected and refluxed on a steam bath with gradual addition of n-hexane and the desired nitrile crystallized from solution, m.p. 141°-143° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04236005
出典データセットuspto-grants-1980_11
ORD IDord-eeabe8c54d2443feb9b80e225e38510f
出典メモuspto-grants-1980_11